Endogenous lipoid pneumonia preceding diagnosis of pulmonary alveolar proteinosis

被引：8

作者：

Antoon, James W. ^{[1
]}

Hernandez, Michelle L. ^{[2
]}

Roehrs, Phillip A. ^{[3
]}

Noah, Terry L. ^{[4
]}

Leigh, Margaret W. ^{[4
]}

Byerley, Julie S. ^{[1
]}

机构：

[1] Univ N Carolina, Sch Med, UNC Hosp, Div Gen Pediat & Adolescent Med, 260 MacNider Bldg,CB 1593, Chapel Hill, NC 27599 USA

[2] Univ N Carolina, Sch Med, UNC Hosp, Div Allergy Immunol Rheumatol & Infect Dis, Chapel Hill, NC USA

[3] Univ N Carolina, Sch Med, Div Hematol & Oncol, UNC Hosp, Chapel Hill, NC USA

[4] Univ N Carolina, Sch Med, Dept Pediat, Div Pulmonol,UNC Hosp, Chapel Hill, NC USA

来源：

CLINICAL RESPIRATORY JOURNAL | 2016年 / 10卷 / 02期

关键词：

crazy paving pattern; interstitial lung disease; lipoid pneumonia; non-specific interstitial pneumonitis; pediatric pulmonology; pulmonary alveolar proteinosis; CHOLESTEROL GRANULOMAS; DISEASE;

D O I：

10.1111/crj.12197

中图分类号：

R56 [呼吸系及胸部疾病];

学科分类号：

摘要：

Pulmonary alveolar proteinosis (PAP) is an under-reported and under-diagnosed condition, with a high percentage of cases found on autopsy or late stage disease. The etiology of PAP includes genetic, primary (anti-granulocyte-macrophage colony-stimulating factor antibodies) and secondary (oncologic, rheumatologic, infectious, chemical and immunologic) causes. Here, we present the first reported pediatric case of endogenous lipoid pneumonia and non-specific interstitial pneumonitis preceding the development of PAP.

引用

页码：246 / 249

页数：4

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